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Arrhythmogenic Cardiomyopathy: Electrical and Structural Phenotypes

Arrhythmogenic Cardiomyopathy: Electrical and Structural Phenotypes

http://www.wikidata.org/entity/Q33167672

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Quantification of Cardiomyocyte Alignment from Three-Dimensional (3D) Confocal Microscopy of Engineered Tissue.Cardiac magnetic resonance imaging: Which information is useful for the arrhythmologist?Right ventricular scar-related ventricular tachycardia in nonischemic cardiomyopathy: Electrophysiological characteristics, mapping, and ablation of underlying heart disease.Arrhythmogenic right ventricular dysplasia/cardiomyopathy: an electrocardiogram-based review.The arrhythmogenic cardiomyopathy-specific coding and non-coding transcriptome in human cardiac stromal cells.Case report of familial sudden cardiac death caused by a DSG2 p.F531C mutation as genetic background when carrying with heterozygous KCNE5 p.D92E/E93X mutation Arrhythmogenic Inflammatory Cardiomyopathy: A Review

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P2860

Arrhythmogenic Cardiomyopathy: Electrical and Structural Phenotypes

http://www.wikidata.org/entity/Q33167672

description

2016 nî lūn-bûn

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2016 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2016 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2016年の論文

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2016年論文

@yue

2016年論文

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2016年論文

@zh-hk

2016年論文

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2016年論文

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2016年论文

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name

Arrhythmogenic Cardiomyopathy: Electrical and Structural Phenotypes

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Arrhythmogenic Cardiomyopathy: Electrical and Structural Phenotypes

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Arrhythmogenic Cardiomyopathy: Electrical and Structural Phenotypes

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Arrhythmogenic Cardiomyopathy: Electrical and Structural Phenotypes

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Arrhythmia & electrophysiology review

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Arrhythmogenic Cardiomyopathy: Electrical and Structural Phenotypes

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Ardan M Saguner

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Corinna Brunckhorst

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Deniz Akdis

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P2860

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy

Suppression of canonical Wnt/beta-catenin signaling by nuclear plakoglobin recapitulates phenotype of arrhythmogenic right ventricular cardiomyopathy

Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene

Treatment of arrhythmogenic right ventricular cardiomyopathy/dysplasia: an international task force consensus statement

TMEM43 mutation p.S358L alters intercalated disc protein expression and reduces conduction velocity in arrhythmogenic right ventricular cardiomyopathy

Rare Disease Terminology and Definitions-A Systematic Global Review: Report of the ISPOR Rare Disease Special Interest Group

Structure and function of desmosomal proteins and their role in development and disease

Arrhythmogenic right ventricular dysplasia/cardiomyopathy: pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right ventricular dysplasia/cardiomyopathy genotype-phenotype follow-up study

Interactions between ankyrin-G, Plakophilin-2, and Connexin43 at the cardiac intercalated disc

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90-101

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scholarly article

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10.15420/AER.2016.4.3

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2

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5

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27617087

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5013177

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